Synthesis of 2-deoxy-β-C-pyranosides by diastereoselective hydrogen atom transfer
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (13) , 1897-1900
- https://doi.org/10.1016/s0040-4039(00)98814-2
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Einfache Synthese von Cβ‐D‐Glucopyranosylaromaten ‐ Synthese des 5,7,4′‐Tri‐O‐methylvitexinsEuropean Journal of Organic Chemistry, 1989
- Funktionell substituierte Vinylcarbanionen, 38. C‐Glucoside durch direkte 1‐C‐Lithiierung von 2‐Phenylsulfinyl‐aktiviertem D‐GlucalEuropean Journal of Organic Chemistry, 1989
- Oxygenated allylic silanes: useful homoenolate equivalents for the stereoselective C-glycosidation of pyranoside derivativesThe Journal of Organic Chemistry, 1989
- Studies on C-Glycosides XIII C-Glucosides from O-Glucosyl 3,5-Dinitro BenzoateSynthetic Communications, 1989
- Stereoselective Syntheses of 2-Deoxy-β-C-arabino- and ribopyranosides: 2-Deoxy-β-arabino- and ribopyranosyl CyanidesBulletin of the Chemical Society of Japan, 1989
- Substitution reactions of 2-benzenesulphonyl cyclic ethers with carbon nucleophilesTetrahedron, 1989
- Direct anomeric substitution of pyranyl esters using organocopper reagentsTetrahedron Letters, 1989
- The Wittig-Horner reaction on 2,3,4,6-tetra-O-benzyl-D-mannopyranose and 2,3,4,6-tetra -O-benzyl-D-glucopyranoseJournal of the Chemical Society, Perkin Transactions 1, 1989
- Stereocontrolled synthesis of C-glycosides by reaction of organocuprates with protected 1,2-anhydro sugars, and their transformation into 2-deoxy-C-glycosidesJournal of the Chemical Society, Chemical Communications, 1989
- A convenient method for replacement of the anomeric hydroxy group in carbohydrates by difluoromethyl functionalityJournal of the Chemical Society, Chemical Communications, 1989